<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Public Health">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>32</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2003</Year>
        <Month>06</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">PCR- Detection of Candida albicans in Blood Using a New Primer Pair to Diagnosis of Systemic Candidiasis</title>
    <FirstPage>1</FirstPage>
    <LastPage>5</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>SH Mirhendi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>K Makimura</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">The opportunistic pathogen C.albicans is able to cause disseminated infections in immunocompromised patients. Microbiological methods for the diagnosis of invasive candidiasis have many problems including low sensitivity, requirement to invasive clinical sampling such as biopsies or multiple blood cultures and need to expertise laboratory stuff. Since PCR has proven to be a powerful tool in the early diagnosis of several infectious diseases, we applied this approach as a rapid and sensitive method in detection of C.albicans cells in blood samples, for establishment a clinically useful method in diagnosing systemic candidiasis. DNA were extracted from blood samples seeded by serially diluted C.albicans cells, by omitting WBC and RBC followed by enzymatic breaking of fungal cell wall and phenol &#x2013; chlorophorm extraction and alcohol precipitation of DNA. A new primer pair was designed for PCR-amplification of a part of ribosomal RNA gene. The primer set was able to amplify all medically important Candida species. When PCR was performed for detection of purified DNA, the sensitivity of the method was about 1 picogram fungal DNA, whereas the sensitivity for detection of C.albicans blastospores inoculated in blood was as few as 10 cell per 0.1 ml of blood. This method could be sensitive and useful for early and rapid diagnosis of systemic Candida infections and to simultaneous detection and speciation of Candida species by PCR-RFLP method.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/1967</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/1967/1948</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>32</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2003</Year>
        <Month>06</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Oxidation of Pentachlorophenol by Fenton&#x2019;s Reagent</title>
    <FirstPage>6</FirstPage>
    <LastPage>10</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>M Farrokhi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>AR Mesdaghinia</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>S Naseri</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>AR Yazdanbakhsh</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Several authors have indicated that PCP is a toxic chemical and recalcitrant to biodegradation. AOPs is one of the moste effective
process for degradation of persistant compound.Since the mineralization of recalcitrant compound by AOPs (Advanced Oxidation
Processes) often requires long reaction time and strong doses of oxidant, the combination of this process with biological one,
considered as an efficient and economic method. In this worke degradation of pentachlorophenol in aqueous solution with fenton
reagent (H2O2 +Ferrous ion)was studied. The experiment was done in batch mode, and the initial concentration of PCP was
0.055mM, in pH=3, H2O2=0.6mM, Fe=0.2mM, more than 95% of PCP was degraded in first minute after the reaction was
started.Therefor this reaction is very fast and in the initial phase degredation of PCP follows first order kinetics and kineticts constant
(K) was 0.026 (S-1). Chloride ion generatation as PCP degredation by product was investigated ,and it was found that the scavenging
effect of chloride is negligible. pH and UV215 absorbance analysis, after reaction completion, indicated that generated intermediates
have the less chlorinated nature, acidic properties and nonphenolic structure. Chloride ion increases from 0 mg/L to 6 mg/L, pH
decreases from 3 to 2.82 and UV215 absorbance decreasees from 0.48 to 0.1, therefor it can be resulted that their biodegradability
modified and their recalcitrance reduced. In the long time reaction (10hr) experiments, TOC and COD analysis indicated that PCP
did not mineralize and TOC and COD reduction was only 20% and 30% respectively. Results from this study indicated that
scavenging effects of generated intermadiate is important in highe doses of H2O2.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/1968</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/1968/1949</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>32</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2003</Year>
        <Month>06</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Detection of Rare and Unknown Mutations in &#xDF;- tathalassemia Traits in Iran</title>
    <FirstPage>11</FirstPage>
    <LastPage>14</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>M Habibi Roudknar</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>H Najmabadi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>P Derakhshandeh</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>DD Farhud</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Beta-thalassemia, by its high frequency and heterogenecity, constitues a real problem of health in Iran. Aboute 13 beta globin
mutations encompass 70-90% of mutations spectrum in Iran, the rest are rare or unknown. In this study six mutations of the codon
IVSI-130(G-C), Fr16 (-C), codon35 (-C), fr23/24(-G), codon8 (+G) and codon 20 (GTG-GAG) were recognized and added to
spectrom of beta globin mutations in Iran, Using ARMS/PCR and DNA sequencing. Three latter cases are reported for first time.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/1969</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/1969/1950</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>32</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2003</Year>
        <Month>06</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Sensitive Detection of Giardia Cysts by Polymerase Chain Reaction (PCR)</title>
    <FirstPage>15</FirstPage>
    <LastPage>18</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>M Nikaeen</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>AR Mesdaghinia</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>M Jeddi Tehrani</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>M Rezaian</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>F Vaezi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Giardia is one of the most common human parasites and causes a lengthly course of nonbacterial diarrhea. Disease outbreaks due to
Giardia infection are often attributed to contaminated water supplies. A major problem associated with detection for this organism is
the lack of sensitive and reliable methods. PCR has the potential to address many of the limitations.We have performed a PCR-based
method for sensitive detection of Giardia cysts. Because the sensitivity of PCR is a function of the efficiency of DNA extraction
from cysts, we have also compared some different methods for DNA extraction from the cysts. Giardia cysts were collected from
infected human, partially purified and serially diluted samples were prepared. DNA was extracted by 3 different methods and we
found that simple repeated freezing and thawing was the best method for extraction of DNA from the cysts. A 163 bp conserved
fragment related to the giardial heat shock protein (HSP70) gene was used as the target for PCR amplification. We were able to
detect as few as 5 cysts in the samples. The results suggest the potential utilities of PCR for sensitive detection of Giardia in water
sources.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/1970</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/1970/1951</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>32</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2003</Year>
        <Month>06</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Survey of Intestinal Parasitic Infection in Leukemic Children and Evaluation of their Serum Immunoglobulins</title>
    <FirstPage>19</FirstPage>
    <LastPage>21</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>MJ Gharavi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>F Ashraf</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>P Vosough</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>MB Rokni</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Infection is one of the cardinal difficulties in the children with acute leukemia and is the leading cause of mortality among them. The prevalence of infection in these patients has several reasons including usage of cytotoxic agents, corticosteriods, broad consumption of antibiotics, duration of confinement in hospital, defective of cellular and humoral Immunity, neutropenia and dysfunction of neutrophils. Despite the fact that intestinal parasitic infection is a rather frequent finding and a health problem in developing countries, in our experience the incidence of helminthic and protozoa infections among children with leukemia was uncommon. Totally 141 patients with leukemia and 70 cases of control group were examined in a period of 12 months, which 40% and 2.8% of former and latter groups, had intestinal pathogen and non-pathogen parasites, respectively. When we compared the frequency of parasitic infection in the control group with the leukemic children, we found no significant difference. It is speculated that parasitic infections may uncommon in these children for numerous reasons such as immunologic and pharmacologic parameters.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/1971</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/1971/1952</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>32</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2003</Year>
        <Month>06</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Distribution of Soft Ticks and Their Infection with Borrelia in Hamadan Province, Iran</title>
    <FirstPage>22</FirstPage>
    <LastPage>24</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>H Vatandoost</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>A Ghaderi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>E Javadian</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>AH Zahir Nia</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>Y Rassi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>N Piazak</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>EB Kia</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>M Shaeghi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>Z Zelmodarreiy</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>M Abolhasani</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Tick-borne diseases like tick-borne relapsing fever are a public health problem in Iran. Its occurrence is more prevalent in north part of country. In order to determine the distribution of soft ticks, Argasidae, and their infection with Borrelia species in Hamadan province, 53 villages were selected randomly. A total of 4805 ticks were collected directly from human dwellings, poultries, and animal shelters. They belong to the genus Argas and Ornithodoros, among which 52.3% were Argas persicus, 2.6% A. reflexus, 2% Ornithodoros canestrinni, 41.4% O. lahorensis, and 1.77% O.tholozani . The most prevalent species was A.persicus and the least one O. lahorensis. Examination of ticks revealed that O.tholozani was infected with Borrelia persica. Infection rate and disease prevalence is coincident in the region. The results will be discussed in more details in terms of preventive measures.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/1972</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/1972/1953</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>32</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2003</Year>
        <Month>06</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Antibacterial Effects of Royal Jelly on Different Strains of Bacteria</title>
    <FirstPage>25</FirstPage>
    <LastPage>30</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>S Eshraghi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>F Seifollahi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Honey and royal jelly are complex heterogeneous mixtures of flower s&#x2019; nectar sugars proteins and bees&#x2019; glandular secretions. Royal
jelly is the hypo-pharyngeal gland excretion of the young worker honeybees (Apis mellifera). The wonderful effects of royal jelly on
the sexual ability and maturity of the queen has been an interesting topic and controversial issue for researchers for many years. The
main purpose of this study was to investigate the anti-bacterial effects of royal jelly against six different bacteria (Escherichia coli,
Staphylococcus aureus, Streptomyces griseus, and three unclassified strains of Streptomyces). Four concentrations of water soluble
extracts of pure royal jelly were prepared and added drop wise to the bacterial strains seed layer cultured individually. Attempt was
made to find out the antibacterial properties of royal jelly by means of agar distribution method (drop-plate). The diameter of the
clean zone formed in each concentration was measured and correlated to the ability of the extracts to inhibit the growth of
microorganisms. Interestingly the results show inhibitory effects of royal jelly on different strains of the bacteria in-vitro. Ethersoluble
and non-soluble fractions of the royal jelly were also examined using the above method. It was found that the antibacterial
effect of ether-soluble fraction is substantially higher than the effect of ether non-soluble fraction. The zones formed by ether-soluble
fractions of royal jelly in the rout of distribution in agar belong to the potency of anti-bacterial properties of fatty acids present in this
fraction of royal jelly (10 -HDA). It was also shown that the non ether-soluble fraction of royal jelly contains a bactericidal substance
called royalisin that was found to have potent antibacterial activity. This fraction of royal jelly revealed weaker anti-bacterial effect
than the ether-soluble fraction and even of pure royal jelly.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/1973</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/1973/1954</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>32</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2003</Year>
        <Month>06</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Prevalence of Intestinal Parasites among Children in Day-care Centers in Damghan - Iran</title>
    <FirstPage>31</FirstPage>
    <LastPage>34</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>A Heidari</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>MB Rokni</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">In order to identify the prevalence of parasitic intestinal infections and to determine the impact of some factors, such as age, health houses, education, environmental health etc, on infection, this survey was carried out on 461 stool specimens and scotch tapes obtained from children resident in day-care centers in Damghan city, Semnan province, Iran. The samples were tested using formalin-ether concentration and Graham methods. The analysis of the results showed that at least 68.1 percent of the individuals tested, were infected with one species of pathogen or non-pathogen parasites. The rate of infection for Enterobius vermicularis, Giardia lamblia, Entamoeba histolytica, Ascaris lumbricoides, Hymenolepis nana, Entamoeba coli, Blastocystis hominis, Iodamoeba butschlii and Chilomastix mesnili was 33.8%, 26.2%, 2.4%, 3%, 4.8%, 5.8%, 4.8%, 2.7% and 4% respectively. A significant difference was seen between the rate of infection and parents&#x2019; education (P&lt;0.005) but was negative regarding age, sex, and health houses. It is concluded that sanitary measurements should be conducted in such centers to decrease the rate of parasitic infection.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/1974</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/1974/1955</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>32</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2003</Year>
        <Month>06</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Interpretation of the Widal Test in Infected Children</title>
    <FirstPage>35</FirstPage>
    <LastPage>37</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>S Noorbakhsh</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>S Rimaz</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>AA Rahbarimanesh</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>S Mamishi</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Typhoid fever is endemic in Iran. Isolation of S. typhi is a gold standard for diagnosis. Laboratory diagnosis of S. typhi infection
relies on serological tests such as the Widal test. This study describes seroprevalence of TO and TH antibody in nonfebrile healthy
and febrile with non-typhoid illness. For detection of sensitivity and specificity of Widal test in typhoidal fever diagnosing Widal test
was performed on serum specimen of the culture-positive cases of typhoid fever in children aged between 1 and14 years in Tehran,
A cross &#x2013;sectional study was carried out. Widal tests were performed on 40 healthy nonfebrile children; 40 patients with non
typhoidal febrile illness and 58 cases with bacteriologically documented typhoid fever specificity, sensitivity, positive and negative
predictive values and the efficacy of the test were determined.
Agglutinin titres &#x2264; 1:40 were considered normal for TO and TH at 96.25% and 93.75% confidence levels, respectively. Titres above
these levels. TO&gt;1:40 and TH&gt;1:40, were considered to be abnormal. 25% of patients showed no response to either agglutinin (TH
and TO); and 44.8% of cases shown no response for TO agglutinin. TO &gt;1/320 was not seen in any cases but TH &gt;1/320 was
detected in 20.6% of cases. Salmonella typhi TO and H agglutinin titers &gt; 1/40 were considered to be significant with 75.86%
sensitivity and 93.75% specificity, respectively. The positive and negative predictive values were 89.79% and 84.26%, respectively.
This study suggests that seroprevalence studies in healthy children can help as validate use for particular serological cut-off point.</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/1975</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/1975/1956</pdf_url>
  </Article>
</Articles>
